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Original Articles

C3‐Symmetric Tripodal Thio/Diglycolamide‐Based Ligands for Trivalent f‐Element Separations

, , , &
Pages 2129-2146 | Received 21 Oct 2005, Accepted 02 Mar 2006, Published online: 15 Feb 2007
 

Abstract

Three new C 3‐symmetric ligands bearing diglycolamide and thiodiglycolamide units on a triphenoxymethane platform have been synthesized and evaluated as trivalent f‐element extractants from nitric acid media. Liquid‐liquid extraction studies of eleven different lanthanides from 1 M nitric acid into dichloromethane revealed a strong influence of the amidic substituents on the extraction efficiency. A comparison of the 1H NMR spectrum of the Lu(III) complex formed with the tris‐DGA ligand and the organic solution after the extraction experiment confirms that all three arms bind the metal during the extraction experiment and form a C 3‐symmetric complex. The newly synthesized lipophilic di‐n‐butyl tris‐diglycolamide was found to be a significantly weaker extractant in comparison to the di‐isopropyl analogs. The distance separating the metal binding groups from the triphenoxymethane platform had little influence on the selectivity or binding efficiency of the ligands. Experiments with the tris‐thiodiglycolamide derivative highlighted the importance of the etheric oxygens for metal binding.

Acknowledgements

The authors gratefully acknowledge financial support from the Nuclear Energy Research Initiative (Grant 02–98) of the Department of Energy (DE‐FG07‐02SF22614). The submitted manuscript has been created by the University of Chicago as Operator of Argonne National Laboratory (“Argonne”) under Contract No. W‐31‐109‐ENG‐38 with the U.S. Department of Energy. The U.S. Government retains for itself, and others acting on its behalf, a paid‐up, nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf of the Government.

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